Case report: Diagnosis of a patient with Sifrim–Hitz–Weiss syndrome, development and epileptic encephalopathy-14, and medium chain acyl-CoA dehydrogenase deficiency

Overview of attention for article published in Frontiers in Pediatrics, September 2023

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New Research: Case report: Diagnosis of a patient with Sifrim–Hitz–Weiss syndrome, development and epileptic encephalopathy-14, and medium chain acyl-CoA dehydrogenase deficiency: Background It is generally recognized that genetic metabolic… #Pediatrics h

05 Oct 2023

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